{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,5]],"date-time":"2026-07-05T21:22:38Z","timestamp":1783286558978,"version":"3.54.6"},"reference-count":11,"publisher":"Elsevier BV","issue":"5","license":[{"start":{"date-parts":[[2019,9,1]],"date-time":"2019-09-01T00:00:00Z","timestamp":1567296000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,9,1]],"date-time":"2019-09-01T00:00:00Z","timestamp":1567296000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","jvoice.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Voice"],"published-print":{"date-parts":[[2019,9]]},"DOI":"10.1016\/j.jvoice.2018.02.002","type":"journal-article","created":{"date-parts":[[2018,7,14]],"date-time":"2018-07-14T12:43:27Z","timestamp":1531572207000},"page":"728-729","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":1,"title":["Botox Injection for Laryngeal Dysfunction in Alexander Disease"],"prefix":"10.1016","volume":"33","author":[{"given":"Amy","family":"Rutt","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Selmin","family":"Karatayli Ozgursoy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jvoice.2018.02.002_bib0010","doi-asserted-by":"crossref","first-page":"161","DOI":"10.1016\/j.jns.2013.05.019","article-title":"Familial adult-onset Alexander disease with a novel mutation (D78N) in the glial fibrillary acidic protein gene with unusual bilateral basal ganglia involvement","volume":"331","author":"Wada","year":"2013","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.jvoice.2018.02.002_bib0015","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1093\/brain\/72.3.373","article-title":"Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant","volume":"72","author":"Alexander","year":"1949","journal-title":"Brain"},{"key":"10.1016\/j.jvoice.2018.02.002_bib0020","doi-asserted-by":"crossref","first-page":"779","DOI":"10.1002\/ana.10375","article-title":"Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease","volume":"52","author":"Namekawa","year":"2002","journal-title":"Ann Neurol"},{"key":"10.1016\/j.jvoice.2018.02.002_bib0025","doi-asserted-by":"crossref","first-page":"2077","DOI":"10.1016\/j.yexcr.2007.04.004","article-title":"GFAP and its role in Alexander disease","volume":"313","author":"Quinlan","year":"2007","journal-title":"Exp Cell Res"},{"key":"10.1016\/j.jvoice.2018.02.002_bib0030","doi-asserted-by":"crossref","first-page":"265","DOI":"10.1001\/archopht.117.2.265","article-title":"Neuro-ophthalmic, radiographic, and pathologic manifestations of adult-onset Alexander disease","volume":"117","author":"Martidis","year":"1999","journal-title":"Arch Ophthalmol"},{"key":"10.1016\/j.jvoice.2018.02.002_bib0035","doi-asserted-by":"crossref","first-page":"49","DOI":"10.1212\/01.wnl.0000438230.33223.bc","article-title":"Neuroimaging and clinical features in type II (late-onset) Alexander disease","volume":"82","author":"Graff-Radford","year":"2014","journal-title":"Neurology"},{"issue":"pt 9","key":"10.1016\/j.jvoice.2018.02.002_bib0040","doi-asserted-by":"crossref","first-page":"2321","DOI":"10.1093\/brain\/awn178","article-title":"Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature","volume":"131","author":"Pareyson","year":"2008","journal-title":"Brain"},{"key":"10.1016\/j.jvoice.2018.02.002_bib0045","doi-asserted-by":"crossref","first-page":"1307","DOI":"10.1001\/archneur.60.9.1307","article-title":"Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene","volume":"60","author":"Stumpf","year":"2003","journal-title":"Arch Neurol"},{"key":"10.1016\/j.jvoice.2018.02.002_bib0050","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1016\/j.jns.2004.07.008","article-title":"Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP","volume":"225","author":"Shiihara","year":"2004","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.jvoice.2018.02.002_bib0055","doi-asserted-by":"crossref","first-page":"5017","DOI":"10.1523\/JNEUROSCI.5384-11.2012","article-title":"Alexander disease","volume":"32","author":"Messing","year":"2012","journal-title":"J Neurosci"},{"key":"10.1016\/j.jvoice.2018.02.002_bib0060","doi-asserted-by":"crossref","first-page":"1366","DOI":"10.1097\/00005537-200008000-00028","article-title":"Botulinum toxin for essential tremor of the voice with multiple anatomical sites of tremor: a crossover design study of unilateral versus bilateral injection","volume":"110","author":"Warrick","year":"2000","journal-title":"Laryngoscope"}],"container-title":["Journal of Voice"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0892199717305684?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0892199717305684?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,11]],"date-time":"2025-10-11T19:34:09Z","timestamp":1760211249000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0892199717305684"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,9]]},"references-count":11,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2019,9]]}},"alternative-id":["S0892199717305684"],"URL":"https:\/\/doi.org\/10.1016\/j.jvoice.2018.02.002","relation":{},"ISSN":["0892-1997"],"issn-type":[{"value":"0892-1997","type":"print"}],"subject":[],"published":{"date-parts":[[2019,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Botox Injection for Laryngeal Dysfunction in Alexander Disease","name":"articletitle","label":"Article Title"},{"value":"Journal of Voice","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jvoice.2018.02.002","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 The Voice Foundation. Published by Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}